HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroaniline → ethyl acetoacetate, sodium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Butanoic acid, 2-ethyl-3-oxo-, ethyl ester | HCID 79065 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Product | ethyl acetoacetate, sodium salt | HCID 85195 | — |
Reaction Steps
The p-chlorophenylhydrazone of ethyl 2-oxobutanoate was prepared by adaptation of the Japp-Klingemann reaction as described by Lions and Hughes (J. Proc. Roy. Soc. N.S. Wales 1939, 71: 445) to p-chloroaniline and ethyl 2-ethylacetoacetate. This phenylhydrazone was treated with HCl-ethanol according to the procedure of Lions and Hughes (J. Proc. Roy. Soc. N.S. Wales 1939, 71: 445) as applied therein to the corresponding bromophenylhydrazone. The title substance was collected by filtration as an orange solid after suspending the concentrated residue in water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06649634B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-5293d7755e5f4c0ca75af02f1701131b |
| Source note | uspto-grants-2003_11 |